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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Class Implantable

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RELINE-O Ti Rod, 5.0x45mm Straight
Nuvasive, Inc.
15350045
In Commercial Distribution

  • 00887517508959 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x40mm Straight
Nuvasive, Inc.
15350040
In Commercial Distribution

  • 00887517508942 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x35mm Straight
Nuvasive, Inc.
15350035
In Commercial Distribution

  • 00887517508935 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x30mm Straight
Nuvasive, Inc.
15350030
In Commercial Distribution

  • 00887517508928 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x25mm Straight
Nuvasive, Inc.
15350025
In Commercial Distribution

  • 00887517508911 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0x20mm Straight
Nuvasive, Inc.
15350020
In Commercial Distribution

  • 00887517508904 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 6.0x170mm Lordotic
Nuvasive, Inc.
14360170
In Commercial Distribution

  • 00887517508829 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 6.0x160mm Lordotic
Nuvasive, Inc.
14360160
In Commercial Distribution

  • 00887517508805 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 6.0x150mm Lordotic
Nuvasive, Inc.
14360150
In Commercial Distribution

  • 00887517508782 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 6.0x140mm Lordotic
Nuvasive, Inc.
14360140
In Commercial Distribution

  • 00887517508768 ()


  • Bone-screw internal spinal fixation system, non-sterile
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